Introducing PLoS Genetics. by Wayne N Frankel

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PLoS Genetics turns three: looking back, looking ahead. by Wayne N Frankel, Gregory S Barsh

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PRAS: Predicting functional targets of RNA binding proteins based on CLIP-seq peaks. by Jianan Lin, Yuping Zhang, Wayne N Frankel, Zhengqing Ouyang

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Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy by Samuel Asinof, Connie Mahaffey, Barbara Beyer, Wayne N. Frankel, Rebecca Boumil

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Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus by Nicole A. Hawkins, Melinda S. Martin, Wayne N. Frankel, Jennifer A. Kearney, Andrew Escayg

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Sensory regulation of absence seizures in a mouse model of Gnb1 encephalopathy by Sasa Teng, Fenghua Zhen, Briana R. McRae, Elaine Zhu, Wayne N. Frankel, Yueqing Peng

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Complex seizure disorder caused by Brunol4 deficiency in mice. by Yan Yang, Connie L Mahaffey, Nathalie Bérubé, Terry P Maddatu, Gregory A Cox, Wayne N Frankel

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Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy. by Wayne N Frankel, Connie L Mahaffey, Tracy C McGarr, Barbara J Beyer, Verity A Letts

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Altered excitatory transmission onto hippocampal interneurons in the IQSEC2 mouse model of X-linked neurodevelopmental disease by Megha Sah, Amy N. Shore, Sabrina Petri, Ayla Kanber, Mu Yang, Matthew C. Weston, Wayne N. Frankel

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CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function. by Jacy L Wagnon, Michael Briese, Wenzhi Sun, Connie L Mahaffey, Tomaž Curk, Gregor Rot, Jernej Ule, Wayne N Frankel

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Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy. by Samuel K Asinof, Stacey J Sukoff Rizzo, Alexandra R Buckley, Barbara J Beyer, Verity A Letts, Wayne N Frankel, Rebecca M Boumil

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A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice. by Rebecca M Boumil, Verity A Letts, Monica C Roberts, Christine Lenz, Connie L Mahaffey, Zhong-Wei Zhang, Tobias Moser, Wayne N Frankel

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DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's disease. by Harriet M Jackson, Kristen D Onos, Keating W Pepper, Leah C Graham, Ellen C Akeson, Candice Byers, Laura G Reinholdt, Wayne N Frankel, Gareth R Howell

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Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor by Sophie Colombo, Haritha P. Reddy, Haritha P. Reddy, Sabrina Petri, Damian J. Williams, Boris Shalomov, Ryan S. Dhindsa, Sahar Gelfman, Daniel Krizay, Amal K. Bera, Mu Yang, Mu Yang, Yueqing Peng, Yueqing Peng, Christopher D. Makinson, Christopher D. Makinson, Christopher D. Makinson, Michael J. Boland, Michael J. Boland, Wayne N. Frankel, Wayne N. Frankel, David B. Goldstein, David B. Goldstein, Nathan Dascal

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Arfgef1 haploinsufficiency in mice alters neuronal endosome composition and decreases membrane surface postsynaptic GABAA receptors by JiaJie Teoh, Narayan Subramanian, Maria Elena Pero, Francesca Bartolini, Ariadna Amador, Ayla Kanber, Damian Williams, Sabrina Petri, Mu Yang, Andrew S. Allen, Jules Beal, Sheryl R. Haut, Wayne N. Frankel

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Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency. by Sarah A Dugger, Ryan S Dhindsa, Gabriela De Almeida Sampaio, Andrew K Ressler, Elizabeth E Rafikian, Sabrina Petri, Verity A Letts, JiaJie Teoh, Junqiang Ye, Sophie Colombo, Yueqing Peng, Mu Yang, Michael J Boland, Wayne N Frankel, David B Goldstein

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meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays. by Sahar Gelfman, Quanli Wang, Yi-Fan Lu, Diana Hall, Christopher D Bostick, Ryan Dhindsa, Matt Halvorsen, K Melodi McSweeney, Ellese Cotterill, Tom Edinburgh, Michael A Beaumont, Wayne N Frankel, Slavé Petrovski, Andrew S Allen, Michael J Boland, David B Goldstein, Stephen J Eglen

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